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How much do associate scientist analytical development jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for associate scientist analytical development in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $40.87 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Scientist Analytical Development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

What are some common challenges an Associate Scientist in Analytical Development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What does an Associate Scientist in Analytical Development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

What is the difference between Associate Scientist Analytical Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

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Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in the United States as of May 2026, with employment types broken down into 11% As Needed, 34% Full Time, 33% Part Time, and 22% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $74,723 per year, or $35.9 per hour.
Scientist, Analytical Development

Scientist, Analytical Development

Avid Bioservices

Tustin, CA

$120K - $135K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

Job description

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
In the Scientist, Analytical Development role you will have the opportunity to focus on developing cell-based, ELISA, HPLC, and/or CE methods and other analytical techniques to identify and characterize protein biologics. This position offers the chance to interface with project management, Process Development, Quality Control, as well as to interface with external clients. The Scientist will lead testing and sampling to support validation, process development, and stability studies in a non-GMP and GMP environment. Individual will take a product through method development and eventual transfer to a quality control department in a GMP environment. They will have a substantial understanding of the job and apply knowledge and skills to complete a wide range of tasks, as well as support and lead continuous improvement initiatives.
Key Responsibilities:
  • Develop, perform, troubleshoot and review routine wet chemistry/ELISA/cell-based immunoassays, electrophoresis (SDS-PAGE/CE/Maurice) and/or HPLC. May be designated as study lead for validation projects, investigations, and method development projects.
  • Must use scientific reasoning when making decisions regarding the quality of the data reported. Expected to research/gather information without supervision and to make scientifically sound decisions based on knowledge and experience.
  • Train/supervise the experimental work of more junior analysts.Tabulate and graph data, and prepare technical reports for senior personnel. Review technical data and reports written by less experienced personnel.
  • Manage client projects and collaboration with other functional areas including but not limited to MFG, QC, and PM. Provide scientific insights for the joint team to make project decisions.
  • Develop, review, revise and write test methods, forms, templates and standard operating procedures and other related documents.
  • Actively support the QC department as the Subject Matter Expert (SME).
  • Knowledge of company cGMPs as well as industry regulations that apply to job functions. Participate in regulatory inspections.
  • Support continuous improvement initiatives.
  • Other tasks as assigned.
Minimum Qualifications:
  • BS degree in Biochemistry, Chemistry, Biology or a related field is required.
  • 8+ years of biotech industry experience working in a QC or analytical lab.
  • Previous experience with analytical testing and equipment utilizing analytical biochemistry methods, writing reports/procedures/specifications, GMPs and regulatory audits required.
  • HPLC, CE, or Potency/ELISA experience is essential.
  • Should have also have experience with protein characterization, electrophoresis, chromatography, and assay validation/qualification.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $120,800 to $135,900 annually, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
Employment Type: Full-Time

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